Pemoline chemical structure
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Cylert

Pemoline (sold as Cylert®) is a medication used to treat attention-deficit hyperactivity disorder (ADHD). Under the Convention on Psychotropic Substances, it is a Schedule IV drug . more...

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Pemoline has some advantages over other stimulants in that it doesn't reduce the appetite or cause dry mouth. However, in some patients Pemoline is suspected of causing liver damage, so regular liver tests are performed are those treated with it. Since receiving FDA aproval in 1975, it has been linked with 21 cases of liver failure, of which 13 resulted in liver replacement or death. In 2005, the FDA withdrew approval for Pemoline due to pressure from certain public advocacy groups. Patient support group the Narcolepsy Network tried to persuade the FDA not to ban it, on the grounds that some patients find all other treatments ineffective or to have dehabilitating side effects. The medication was used by an estimated 10,000 Americans afflicted with narcolepsy.

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Stimulants similarly effective for ADHD
From Journal of Family Practice, 9/1/05 by R.T. Brown

Brown RT, Amler RW, Freeman WS, et al. Treatment of attention-deficit/hyperactivity disorder: overview of the evidence. Pediatrics 2005; 115:749-757.

* Clinical Question

Which drug therapy is more effective in children with attention-deficit hyperactivity disorder?

* Bottom Line

Stimulants have the best evidence of effectiveness in the treatment of children with attention-deficit hyperactivity disorder (ADHD). The research does not give us a clear-cut choice among the stimulants or their formulations, so an empirical, trial-and-error approach is needed. Antidepressants may not be as effective. Behavioral therapy may add benefit to drug therapy, but is less effective than drug therapy when used alone. The role of atomoxetine (Strattera) is unclear because of few comparative studies or long-term studies. (Level of evidence [LOE]=1a)

Study Design

Systematic review

Setting

Various (meta-analysis)

Synopsis

This report is from the American Academy of Pediatrics' Committee on Quality Improvement Subcommittee on Attention-Deficit/Hyperactivity Disorder. It is based on 3 evidence reviews performed by the McMaster Evidence-Based Practice Center, the Canadian Coordinating Office for Health Technology Assessment, the Multimodal Treatment Study for Children with ADHD, and the mysterious "supplemental reviews conducted by the subcommittee."

The McMaster review seems to be the foundation for the report and is a well-described systematic review. Most of the results currently available are from short-term studies that compared the major stimulants used for ADHD. Since the definition of what constitutes "improvement" varies among patients and research studies, study results could not be combined. Studies were not able to show, on average, a difference in treatment between methylphenidate (Ritalin), dextroamphetamine or its individual isomers, and pemoline (Cylert), or a difference in any formulations of the same drug. Similarly, there is no difference in the likelihood of adverse effects, though the studies are small.

Studies of the antidepressants desipramine and imipramine compared with placebo show heterogeneous results. Nonpharmacologic intervention was not as effective as drug therapy, though behavioral therapy enhanced drug therapy in the Multimodal Treatment Study. Regarding the nonstimulant atomoxetine, in a short-term study it is as effective as methylphenidate, with similar side-effect profiles, causing similar appetite suppression and initial weight loss. It doesn't worsen insomnia but can cause daytime drowsiness and increase blood pressure in some adults and children. Atomoxetine has a slow onset of action, taking up to 1 week to begin working, but seems to last longer throughout the day when it does work.

COPYRIGHT 2005 Dowden Health Media, Inc.
COPYRIGHT 2005 Gale Group

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